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Ion Mobility-Enhanced LA-REIMS Improves Molecular Resolution in Ambient Biofluid Metabolomics

Plekhova, V.; Van de Velde, N.; VandenBerghe, A.; Diana Di Mavungu, J.; Vanhaecke, L.

2026-03-12 biochemistry
10.64898/2026.03.10.709786 bioRxiv
Show abstract

Ambient metabolomics techniques such as laser-assisted rapid evaporative ionization mass spectrometry (LA-REIMS) enable fast, preparation-free fingerprinting of biological samples but are inherently limited by spectral congestion in the absence of chromatographic separation. While ion mobility spectrometry provides additional gas-phase separation, maintaining ion transmission under the transient signals characteristic of laser desorption, remains analytically challenging. Here, we define operating conditions for cyclic traveling-wave ion mobility spectrometry (cIMS) that preserve transmission under LA-REIMS duty-cycle constraints and systematically evaluate how cIMS integration reshapes biofluid fingerprints and enhances chemical specificity in chromatography-free metabolomics analysis. Under optimized single-pass conditions, cIMS separation reorganized LA-REIMS spectra into structured mass/mobility feature domains, enabling selective mobility-based filtering of matrix-derived salt cluster ions. This reduced non-biological background contributions by up to 35% of total spectral intensity while preserving over 90% of detected untargeted features. Although cIMS operation introduced a sensitivity penalty relative to time-of-flight-only acquisition, approximately 80% of the total ion current was recovered under optimized conditions. Mobility-resolved data revealed coherent homologous series and class-specific structural trends, particularly for lipids, supporting class-level annotation. Analysis of 101 metabolite and lipid standards covering a broad physicochemical range (logP -5.30 to 19.40) demonstrated comprehensive molecular coverage, high mass accuracy (mean 2.4 ppm), and good agreement with reference CCS values (mean deviation 4.0%), with isomer separation observed for biologically important secondary bile acids in extended separation cycles. Collectively, these results establish LA-REIMS-cIMS as a practical analytical strategy for enhancing chemical specificity and spectral interpretability in support of high-throughput large-scale metabolic fingerprinting. O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=147 SRC="FIGDIR/small/709786v1_ufig1.gif" ALT="Figure 1"> View larger version (42K): org.highwire.dtl.DTLVardef@18a2dfdorg.highwire.dtl.DTLVardef@d165d6org.highwire.dtl.DTLVardef@1750291org.highwire.dtl.DTLVardef@fbbce9_HPS_FORMAT_FIGEXP M_FIG O_FLOATNOGraphical abstractC_FLOATNO Ion mobility spectrometry adds an orthogonal gas-phase separation to LA-REIMS, reorganizing complex biofluid spectra into distinct mass-mobility feature bands and improving molecular resolution in rapid ambient ionization metabolomics. C_FIG

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